Ken Arita

Oncostatin M Receptor-β Mutations Underlie Familial Primary Localized Cutaneous Amyloidosis

Ken Arita, Andrew P. South, Günter Hans‐Filho et al. · The American Journal of Human Genetics · 2008 · 138 citations · Full text

Autoimmune Disease, Immunology, Pathology +4

Colocalization of Kindlin-1, Kindlin-2, and Migfilin at Keratinocyte Focal Adhesion and Relevance to the Pathophysiology of Kindler Syndrome

J.E. Lai-Cheong, Siegfried Ussar, Ken Arita et al. · Journal of Investigative Dermatology · 2008 · 91 citations · Full text

Cell Adhesion, Pathology, Kindler Syndrome +6

Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis

Ming‐Wei Lin, Ding-Dar Lee, Tze Tze Liu et al. · European Journal of Human Genetics · 2009 · 64 citations · Full text

Autoimmune Disease, Immunology, Pathology +3

Plectin deficiency leads to both muscular dystrophy and pyloric atresia in epidermolysis bullosa simplex

Ken Natsuga, Wataru Nishie, Satoru Shinkuma et al. · Human Mutation · 2010 · 60 citations · Full text

Patients with Recessive Dystrophic Epidermolysis Bullosa Develop Squamous-Cell Carcinoma Regardless of Type VII Collagen Expression

Céline Pourreyron, G. S. Cox, Xin Mao et al. · Journal of Investigative Dermatology · 2007 · 57 citations · Full text

Tumor Biology, Medicine, Cutaneous Biology +7